Variant #0000692535 (NC_000017.10:g.80885776A>G, NC_000017.10(NM_005993.4):c.2610-5A>G (TBCD))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.80885776A>G
DNA change (hg38) -
Published as TBCD(NM_005993.4):c.2610-5A>G
ISCN -
DB-ID TBCD_000036
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBCD NM_005993.4 -?/. - c.2610-5A>G r.spl? p.?
ZNF750 NM_024702.2 -?/. - c.-88156T>C r.(?) p.(=)


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